Molecular insights into the transformation of dissolved organic matter during hyperthermophilic composting using ESI FT-ICR MS

被引:55
作者
Yu, Zhen [1 ]
Liu, Xiaoming [1 ]
Chen, Changya [2 ]
Liao, Hanpeng [3 ]
Chen, Zhi [3 ]
Zhou, Shungui [1 ,3 ]
机构
[1] Guangdong Inst Ecoenvironm Sci & Technol, Guangdong Key Lab Integrated Agroenvironm Pollut, Guangzhou 510650, Guangdong, Peoples R China
[2] Hunan Univ Humanities Sci & Technol, Sch Mat & Environm Engn, Hunan Prov Key Lab Fine Ceram & Powder Mat, Loudi 417000, Peoples R China
[3] Fujian Agr & Forestry Univ, Coll Resources & Environm, Fujian Prov Key Lab Soil Environm Hlth & Regulat, Fuzhou 350002, Peoples R China
关键词
Fourier transform ion cyclotron resonance mass spectrometry; Hyperthermophilic composting; Dissolved organic matter; Molecular composition; Humification mechanism; EEM-PARAFAC; SUBSTANCES; EMISSIONS;
D O I
10.1016/j.biortech.2019.122007
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
The aim of this work was to study the molecular compositional changes of dissolved organic matter (DOM) during hyperthermophilic composting (HTC) using electrospray ionization coupled with Fourier transform ion cyclotron resonance mass spectrometry. Our results reveal that DOM in hyperthermophilic compost mainly consisted of lignins/carboxylic-rich alicyclic molecules (72%) with relatively lower H/C (1.24), and the higher double bound equivalent (5.98) and aromaticity index (0.22) when compared with the DOM in composting materials, suggesting that HTC led to an increase in carboxyl-rich, unsaturated, and aromatic compounds. Profiles of the DOM's transformation indicated that low O/C (O/C < 0.3) and high H/C (H/C < 1.5) compounds were preferentially decomposed in the hyperthermophilic phase of HTC. Abundant produced intermediates, such as lignin phenols and amino sugars, were further transformed to refractory humic substances. This investigation extends the current understanding of the molecular mechanisms on humification of HTC, and reveals further applications for hyperthermophilic compost.
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页数:5
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